NM_001372051.1(CASP8):c.706T>C (p.Cys236Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002886729.2
Allele description [Variation Report for NM_001372051.1(CASP8):c.706T>C (p.Cys236Arg)]
NM_001372051.1(CASP8):c.706T>C (p.Cys236Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Or5d38 olfactory receptor family 5 subfamily D member 38 [Mus musculus]
Or5d38 olfactory receptor family 5 subfamily D member 38 [Mus musculus]Gene ID:258644Gene
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Last Updated: Sep 29, 2024